Literature DB >> 30272672

Standardized Measurement of Nasal Membrane Transepithelial Potential Difference (NPD).

George M Solomon1, Inez Bronsveld2, Kathryn Hayes3, Michael Wilschanski4, Paola Melotti5, Steven M Rowe1, Isabelle Sermet-Gaudelus6.   

Abstract

We describe a standardized measurement of nasal potential difference (NPD). In this technique, cystic fibrosis transmembrane conductance regulator (CFTR) and the epithelial sodium channel (ENaC) function are monitored by the change in voltage across the nasal epithelium after the superfusion of solutions that modify ion channel activity. This is enabled by the measurement of the potential difference between the subcutaneous compartment and the airway epithelium in the nostril, utilizing a catheter in contact with the inferior nasal turbinate. The test allows the measurement of the stable baseline voltage and the successive net voltage changes after perfusion of 100 µM amiloride, an inhibitor of Na+ reabsorption in Ringer's solution; a chloride-free solution containing amiloride to drive chloride secretion and 10 µM isoproterenol in a chloride-free solution with amiloride to stimulate the cyclic adenosine monophosphate (cAMP)-dependent chloride conductance related to CFTR. This technique has the advantage of demonstrating the electrophysiological properties of two key components establishing the hydration of the airway surface liquid of the respiratory epithelium, ENaC, and CFTR. Therefore, it is a useful research tool for phase 2 and proof of concept trials of agents that target CFTR and ENaC activity for the treatment of cystic fibrosis (CF) lung disease. It is also a key follow-up procedure to establish CFTR dysfunction when genetic testing and sweat testing are equivocal. Unlike sweat chloride, the test is relatively more time consuming and costly. It also requires operator training and expertise to conduct the test effectively. Inter- and intra-subject variability has been reported in this technique especially in young or uncooperative subjects. To assist with this concern, interpretation has been improved through a recently validated algorithm.

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Year:  2018        PMID: 30272672      PMCID: PMC6235174          DOI: 10.3791/57006

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  27 in total

1.  Nasal potential difference measurements in diagnosis of cystic fibrosis: an international survey.

Authors:  Lutz Naehrlich; Manfred Ballmann; Jane Davies; Nico Derichs; Tanja Gonska; Lena Hjelte; Silke van Konigsbruggen-Rietschel; Teresinha Leal; Paola Melotti; Peter Middleton; Burkhard Tümmler; Francois Vermeulen; Michael Wilschanski
Journal:  J Cyst Fibros       Date:  2013-09-07       Impact factor: 5.482

2.  An international randomized multicenter comparison of nasal potential difference techniques.

Authors:  George M Solomon; Michael W Konstan; Michael Wilschanski; Joanne Billings; Isabelle Sermet-Gaudelus; Frank Accurso; François Vermeulen; Elina Levin; Heather Hathorne; Ginger Reeves; Gina Sabbatini; Aubrey Hill; Nicole Mayer-Hamblett; Melissa Ashlock; John Paul Clancy; Steven M Rowe
Journal:  Chest       Date:  2010-05-14       Impact factor: 9.410

Review 3.  The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel.

Authors:  B J Rosenstein; G R Cutting
Journal:  J Pediatr       Date:  1998-04       Impact factor: 4.406

Review 4.  CFTR biomarkers: time for promotion to surrogate end-point.

Authors:  K De Boeck; L Kent; J Davies; N Derichs; M Amaral; S M Rowe; P Middleton; H de Jonge; I Bronsveld; M Wilschanski; P Melotti; I Danner-Boucher; S Boerner; I Fajac; K Southern; R A de Nooijer; A Bot; Y de Rijke; E de Wachter; T Leal; F Vermeulen; M J Hug; G Rault; T Nguyen-Khoa; C Barreto; M Proesmans; I Sermet-Gaudelus
Journal:  Eur Respir J       Date:  2012-08-09       Impact factor: 16.671

5.  Influence of perfusate temperature on nasal potential difference.

Authors:  Inez Bronsveld; François Vermeulen; Dorotha Sands; Teresinha Leal; Anissa Leonard; Paola Melotti; Yasmin Yaakov; Roel de Nooijer; Kris De Boeck; Isabelle Sermet; Michael Wilschanski; Peter G Middleton
Journal:  Eur Respir J       Date:  2012-10-25       Impact factor: 16.671

6.  Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis.

Authors:  Thierry Bienvenu; Isabelle Sermet-Gaudelus; Pierre-Regis Burgel; Dominique Hubert; Bruno Crestani; Laurence Bassinet; Daniel Dusser; Isabelle Fajac
Journal:  Am J Respir Crit Care Med       Date:  2010-02-18       Impact factor: 21.405

7.  A CFTR corrector (lumacaftor) and a CFTR potentiator (ivacaftor) for treatment of patients with cystic fibrosis who have a phe508del CFTR mutation: a phase 2 randomised controlled trial.

Authors:  Michael P Boyle; Scott C Bell; Michael W Konstan; Susanna A McColley; Steven M Rowe; Ernst Rietschel; Xiaohong Huang; David Waltz; Naimish R Patel; David Rodman
Journal:  Lancet Respir Med       Date:  2014-06-24       Impact factor: 30.700

8.  Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis.

Authors:  M Knowles; J Gatzy; R Boucher
Journal:  N Engl J Med       Date:  1981-12-17       Impact factor: 91.245

9.  A multicenter study of the effect of solution temperature on nasal potential difference measurements.

Authors:  Michael P Boyle; Marie Diener-West; Laura Milgram; Michael Knowles; Carla Foy; Pamela Zeitlin; Thomas Standaert
Journal:  Chest       Date:  2003-08       Impact factor: 9.410

10.  Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation.

Authors:  Frank J Accurso; Steven M Rowe; J P Clancy; Michael P Boyle; Jordan M Dunitz; Peter R Durie; Scott D Sagel; Douglas B Hornick; Michael W Konstan; Scott H Donaldson; Richard B Moss; Joseph M Pilewski; Ronald C Rubenstein; Ahmet Z Uluer; Moira L Aitken; Steven D Freedman; Lynn M Rose; Nicole Mayer-Hamblett; Qunming Dong; Jiuhong Zha; Anne J Stone; Eric R Olson; Claudia L Ordoñez; Preston W Campbell; Melissa A Ashlock; Bonnie W Ramsey
Journal:  N Engl J Med       Date:  2010-11-18       Impact factor: 176.079

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  5 in total

1.  Gaming Console Home-Based Exercise for Adults with Cystic Fibrosis: Study Protocol.

Authors:  John D Lowman; George M Solomon; Steven M Rowe; Hon K Yuen
Journal:  Int J Caring Sci       Date:  2020 Spring/Summer

2.  ENaC-mediated sodium influx exacerbates NLRP3-dependent inflammation in cystic fibrosis.

Authors:  Thomas Scambler; Heledd H Jarosz-Griffiths; Daniel Peckham; Michael F McDermott; Samuel Lara-Reyna; Shelly Pathak; Chi Wong; Jonathan Holbrook; Fabio Martinon; Sinisa Savic
Journal:  Elife       Date:  2019-09-18       Impact factor: 8.140

Review 3.  Assays of CFTR Function In Vitro, Ex Vivo and In Vivo.

Authors:  Anabela Santo Ramalho; Mieke Boon; Marijke Proesmans; François Vermeulen; Marianne S Carlon; Kris De Boeck
Journal:  Int J Mol Sci       Date:  2022-01-27       Impact factor: 5.923

Review 4.  Research advances in molecular mechanisms underlying the pathogenesis of cystic fibrosis: From technical improvement to clinical applications (Review).

Authors:  Tao Wei; Hongshu Sui; Yanping Su; Wanjing Cheng; Yunhua Liu; Zilin He; Qingchao Ji; Changlong Xu
Journal:  Mol Med Rep       Date:  2020-10-16       Impact factor: 2.952

5.  Ocular Surface Potential Difference Measured in Human Subjects to Study Ocular Surface Ion Transport.

Authors:  Neel D Pasricha; Alex J Smith; Marc H Levin; Julie M Schallhorn; Alan S Verkman
Journal:  Transl Vis Sci Technol       Date:  2020-10-15       Impact factor: 3.283

  5 in total

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